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The Study of Omega-3 supplementation Effect on Lipid Profiles in Hemodialysis Patients

The Study of Omega-3 supplementation Effect on Lipid Profiles in Hemodialysis Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013081214333N1
Enrollment
60
Registered
2013-09-17
Start date
2013-08-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hemodialysis patients. End-stage renal disease

Interventions

Intervention 1: daily prescription of 1000 mg of omega-3 capsule for 10 weeks to the study group. Intervention 2: daily prescription of one placebo capsule containing sunflower oil to the control grou
Treatment - Drugs
daily prescription of 1000 mg of omega-3 capsule for 10 weeks to the study group
daily prescription of one placebo capsule containing sunflower oil to the control group for 10 weaks

Sponsors

Vice Chancellor for Research Affairs, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criterias: patient's willingness to cooperate, and at least 6 months of dialysis starting time. Exclusion criterias: presence of bleeding and warfarin anticoagulation drugs usage or anti-thrombotic (aspirin, ticlopidine, dipyridamole and clopidogrel); diabetes; hepatitis, and other infectious diseases; body mass index less than 18.5 or more than 30 kg/ m2; steroidal and non-steroidal anti-inflammatory drugs; omega-3 fatty acids supplements and vitamins E or C within two months before the study .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cholestrol. Timepoint: week,0,10. Method of measurement: by cell counter.;Triglycerid. Timepoint: week,0,10. Method of measurement: by sell counter.;H.d.L. Timepoint: week,0,10. Method of measurement: by cell counter.;L.D.L. Timepoint: week,0,10. Method of measurement: by cell counter.;Serum alboumin. Timepoint: weak ,0,10. Method of measurement: by sell counter.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026